"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SNHG31"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 931786	NM_173076.3(ABCA12):c.7715A>G (p.Tyr2572Cys)	ABCA12, SNHG31 (Y2254C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 2861	NM_173076.3(ABCA12):c.7093G>A (p.Asp2365Asn)	ABCA12, SNHG31 (D2047N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign/Likely benign